GMP Training Courses - Regulatory Affairs

Drug Master File Procedures in the EU, the US and Japan

Copenhagen, Denmark

17/18 September 2019

Drug Master File Procedures in the EU, the US and Japan

Plastic/Elastomeric Materials for Pharmaceutical Packaging and Production

Barcelona, Spain

25/26 September 2019

Plastic/Elastomeric Materials for Pharmaceutical Packaging and Production

Change Control -  New Aspects and Best Practices

Heidelberg, Germany

8-9 October 2019

Change Control - New Aspects and Best Practices

How to provide process validation data in regulatory submissions

Hamburg, Germany

29/30 October 2019

How to provide process validation data in regulatory submissions

Webinar: Update IMPs

Heidelberg, Germany

Wednesday, 13 November 2019 14.00 - 15.30 h

Webinar: Update IMPs

Pharmaceutical Contracts: GMP and Legal Compliance

Barcelona, Spain

11/12 February 2020

Pharmaceutical Contracts: GMP and Legal Compliance

Global registration and Life Cycle Management for APIs

Vienna, Austria

10-12 March 2020

Global registration and Life Cycle Management for APIs

Handling Changes and Variations

Heidelberg, Germany

21/22 April 2020

Handling Changes and Variations

How to write the Quality Part of an IMPD

Praha, Czech Republic

13/14 May 2020

How to write the Quality Part of an IMPD

API Regulatory Starting Materials

Hamburg, Germany

26/27 May 2020

API Regulatory Starting Materials

GMP meets Regulatory Affairs

Hamburg, Germany

28/29 May 2020

GMP meets Regulatory Affairs

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